Abstract 282P
Background
Pembrolizumab in combination with neo-adjuvant chemotherapy is a new standard in non-metastatic triple negative breast cancers (TNBC). Most patients with non-metastatic TNBC will survive. Preclinical data show a reduction in the number of primordial follicles following exposure to pembrolizumab. Anti-Müllerian Hormone (AMH) is used to determine ovarian reserve, and its level decreases by almost 90% after exposure to chemotherapy in young breast cancer patients. We sought to assess the impact of pembrolizumab on AMH values in young TNBC patients.
Methods
In this monocentric retrospective study, we included TNBC patients under 43 years of age for whom plasma samples were available before and after treatment. We assessed their AMH, FSH and oestradiol values before (baseline) and at the end of exposure to carboplatin/paclitaxel/epirubicin/cyclophosphamide plus pembrolizumab (P-CT group). These results were compared with those of a retrospective cohort of early TNBC patients under 43 years of age, treated with cyclophosphamide/anthracycline/taxanes but without pembrolizumab (No P group).
Results
Thirteen patients were included in the P-CT group and compared with 67 patients in the No P group. Median age (35y) and BMI (23 kg/m2) were comparable in both groups. Baseline AMH was 1.08 ng/mL in the P-CT group, and 1.4 ng/mL in the No P group (p=0.2). One year after the start of treatment, AMH fell significantly to 0.015 ng/mL (p<0.001 vs baseline) and 0.018 ng/mL (p<0.001), in the P-CT and No P groups, respectively. Notably, 5/13 patients (38%) had undetectable AMH (<0.01 ng/mL) after treatment in the P-CT group and 23/67 (34%) in the No P group. At baseline, no differences were observed between the two groups in FSH and oestradiol values. FSH increased significantly (p<0.001), and oestradiol tended to decrease significantly (p=0.07) after exposure to treatment, with no difference between the P-CT and No P groups.
Conclusions
In this cohort, no impact of the addition of pembrolizumab to standard chemotherapy on the evolution of AMH, FSH or oestradiol before and after treatment was observed in young TNBC patients.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
Centre Henri Becquerel.
Funding
Has not received any funding.
Disclosure
F. Clatot: Financial Interests, Personal, Advisory Board: Merck, BMS, MSD, Gilead, AstraZeneca, Novartis, Daiichi, Roche, Eli Lilly. All other authors have declared no conflicts of interest.
Resources from the same session
312P - Early detection of metastatic disease in asymptomatic early-stage breast cancer patients using imaging: A cross-sectional analytic study at a tertiary hospital
Presenter: John kelvin Lalusis
Session: Poster session 14
313P - A longitudinal follow-up study on the prognosis of patients with breast cancer with delayed diagnosis during the COVID-19 pandemic
Presenter: Jae Pak Yi
Session: Poster session 14
314P - The impact of changes in tumor mutational landscape during neoadjuvant therapy on tumor-informed ctDNA testing in breast cancer patients
Presenter: Mark Magbanua
Session: Poster session 14
315P - Long-term tamoxifen benefit in pre- and postmenopausal patients of high and low risk with luminal A and B breast cancer
Presenter: Oscar Danielsson
Session: Poster session 14
316P - Differential long-term benefit of 2-year adjuvant tamoxifen therapy for luminal-type breast cancer: Insights from a 20-year follow-up analysis of the STO trials
Presenter: Magdalena Rios Romero
Session: Poster session 14
317TiP - A randomized, multicenter, open-label phase II neoadjuvant study to evaluate the safety and efficacy of HER2-ADC disitamab vedotin in combination toripalimab or sequence chemotherapy in participants with HR-negative, HER2 low-expressing breast cancer
Presenter: Zhimin Shao
Session: Poster session 14
318TiP - Neoadjuvant trastuzumab, pertuzumab and tucatinib without chemotherapy in stage II-III HER2-positive breast cancer: The TRAIN-4 study
Presenter: Fleur Louis
Session: Poster session 14
319TiP - NeoBREASTIM: A phase II study of atezolizumab plus RP1 oncolytic immunotherapy in the neoadjuvant setting of triple-negative breast cancer (TNBC)
Presenter: Etienne Bastien
Session: Poster session 14
321P - Sentinel lymph node biopsy in clinical T3-4c breast cancer: A retrospective multicenter cohort study
Presenter: Yasuaki Sagara
Session: Poster session 14
322P - Incidence patterns for locally advanced operable breast cancer by receptor status: SEER 2010-2021
Presenter: Alexandra Thomas
Session: Poster session 14